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Cat. No.: HY-149705

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ICMT-IN-7

ICMT-IN-7 (compound 74) is an inhibitor of ICMT (IC₅₀=0.015 μM). ICMT-IN-7 dose-dependently induces ICMT accumulation in the cytoplasm of HCT-116 cells and inhibits the proliferation of multiple cancer cell lines expressing K-Ras and N-Ras.

For research use only. We do not sell to patients.

CAS No.: 1313603-21-2
Formula: C₂₃H₃₁NO
Molecular Weight:337.50

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (269 KB)

ICMT-IN-7 Chemical Structure

CAS No.: 1313603-21-2

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Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- IC₅₀ & Target
- Cellular Effect
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

IC₅₀ & Target

IC50: 0.015 μM (ICMT)^[1]

Cellular Effect

Cell Line	Type	Value	Description	References
CCRF-CEM	GI₅₀	3 μM Compound: 74	Cytotoxicity against human CCRF-CEM cells expressing K-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay Cytotoxicity against human CCRF-CEM cells expressing K-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay	[PMID: 21661760]
DU-145	GI₅₀	76 μM Compound: 74	Cytotoxicity against human DU145 cells expressing wild type Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay Cytotoxicity against human DU145 cells expressing wild type Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay	[PMID: 21661760]
HCT-116	GI₅₀	26 μM Compound: 74	Cytotoxicity against human HCT116 cells expressing K-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay Cytotoxicity against human HCT116 cells expressing K-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay	[PMID: 21661760]
HL-60	GI₅₀	9 μM Compound: 74	Cytotoxicity against human HL60 cells expressing N-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay Cytotoxicity against human HL60 cells expressing N-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay	[PMID: 21661760]
MIA PaCa-2	GI₅₀	12 μM Compound: 74	Cytotoxicity against human MIAPaCa2 cells expressing K-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay Cytotoxicity against human MIAPaCa2 cells expressing K-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay	[PMID: 21661760]
PC-3	GI₅₀	17 μM Compound: 74	Cytotoxicity against human PC3 cells expressing wild type Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay Cytotoxicity against human PC3 cells expressing wild type Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay	[PMID: 21661760]
SK-MEL-2	GI₅₀	>100 μM Compound: 74	Cytotoxicity against human SK-MEL-2 cells expressing K-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay Cytotoxicity against human SK-MEL-2 cells expressing K-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay	[PMID: 21661760]
T-24	GI₅₀	43 μM Compound: 74	Cytotoxicity against human T24 cells expressing N-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay Cytotoxicity against human T24 cells expressing N-Ras assessed as growth inhibition after 7 days by luminescence-based ATPlite assay	[PMID: 21661760]

Chemical Information

CAS No. 1313603-21-2
Molecular Weight 337.50
Formula C₂₃H₃₁NO
SMILES

CC(C1)(C)OC(C)(C)CC1(CCNC2=CC=CC=C2)C3=CC=CC=C3
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (269 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Judd WR, et al. Discovery and SAR of methylated tetrahydropyranyl derivatives as inhibitors of isoprenylcysteine carboxyl methyltransferase (ICMT). J Med Chem. 2011 Jul 28;54(14):5031-47. [Content Brief]

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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